Basic Research
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Feb 15, 2003; 9(2): 316-319
Published online Feb 15, 2003. doi: 10.3748/wjg.v9.i2.316
Inhibition on the production of collagen type I, III of activated hepatic stellate cells by antisense TIMP-1 recombinant plasmid
Wen-Bin Liu, Chang-Qing Yang, Wei Jiang, Yi-Qing Wang, Jing-Sheng Guo, Bo-Ming He, Ji-Yao Wang
Wen-Bin Liu, Chang-Qing Yang, Wei Jiang, Yi-Qing Wang, Jing-Sheng Guo, Bo-Ming He, Ji-Yao Wang, Division of Gastroenterology, Zhongshan Hospital, Fudan University, Shanghai 200032, China
Author contributions: All authors contributed equally to the work.
Supported by the National Natural Scientific Foundation of China, No. 39970339
Correspondence to: Professor Ji-Yao Wang, Division of Gastroenterology, Zhongshan Hospital, Fudan University, Shanghai 200032, China. jiyao_wang @ hotmail.com
Telephone: +86-21-64041990 Ext 2420 Fax: +86-21-34160980
Received: September 14, 2002
Revised: October 4, 2002
Accepted: October 18, 2002
Published online: February 15, 2003
Abstract

AIM: To investigate the inhibition effects on the production of collagen type I, III secreted by activated rat hepatic stellate cells (rHSCs) by antisense tissue inhibitors of metalloproteinase 1 (TIMP-1) recombinant plasmid through elevating interstitial collagenase activity.

METHODS: rHSCs were extracted from normal rat liver by pronase and collagenase digestion and purified by centrifugal elutriation, and were cultured on plastic dishes until they were activated to a myofibroblastic phenotype after 7-10 d. RT-Nest-PCR and gene recombinant techniques were used to construct the rat antisense TIMP-1 recombinant plasmids which can express in eucaryotic cells. The recombinant plasmid and the pcDNA3 empty plasmid were transfected in rHSCs by Effectene (QIAGEN) separately. Cells were selected after growing in DMEM containing 400 μg/mL G418 for 2-3 wk. Expression of exogenous gene was assessed by Northern blot, and expression of TIMP-1 in rHSCs was determined by Northern blot and Western blot. We tested the interstitial collagenase activity with FITC-labled type I collagen as substrate. Ultimately, we quantified the type I, III collagen by Western blot.

RESULTS: The exogenous antisense TIMP-1 recombinant plasmid could be expressed in rHSCs well, which could block the expression of TIMP-1 greatly, the ratio of TIMP-1/GAPDH was 0.67, 2.41, and 2.97 separately at mRNA level (P < 0.05); the ratio of TIMP-1/β-actin was 0.31, 0.98 and 1.32 separately at protein level (P < 0.05); It might elevate active and latent interstitial collagenase activity, the collagenase activity was 0.3049, 0.1411 and 0.1196 respectively. (P < 0.05), which led to promotion the degradation of type I, III collagen, the ratio of collagen I/β-actin was 0.63, 1.78 and 1.92 separately (P < 0.05); and the ratio of collagen III/β-actin was 0.59, 1.81 and 1.98 separately (P < 0.05).

CONCLUSION: These data shows that the antisense TIMP-1 recombinant plasmid has the inhibitory effects on the production of type I, III collagens secreted by activated rHSCs in vitro. It could be a novel method to reverse hepatic fibrosis in the future.

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